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作 者:王天叫[1] 杨善民[1] 黄宗平[2] 李祺福[2] 李庆阁[2] 周红[1] 郑荣梁[3] 贾忠健[3]
机构地区:[1]厦门大学抗癌研究中心 [2]厦门大学生物系,厦门361005 [3]兰州大学生物系,兰州730000
出 处:《实验生物学报》1999年第4期321-327,共7页Acta Biologiae Experimentalis Sinica
基 金:福建省自然科学基金~~
摘 要:不同时间、不同浓度的isoverbascoside体外处理HL-60细胞,以形态改变(光镜和透射电镜观察)、功能分化(化学发光检测吞噬能力)、恶性度降低(裸鼠成瘤试验)等指标观察其诱导分化作用;以台盼蓝拒染作用和电镜下形态变化确定其细胞毒作用;用流式细胞术测定其对HL-60细胞周期的影响。20—25μmol/L Isov 1—3天诱导HL-60细胞向粒系方向分化,细胞吞噬能力提高,裸鼠成瘤性降低。30—35μmol/L Isov 2—3天对HL-60细胞有强烈的细胞毒作用。20μmol/L Isov处理12h可引起HL-60细胞的G_1期阻滞,在72h时引起HL-60细胞的G_2/M期的阻滞。HL-60 cells were treated by isoverbascoside with different time and different concentrations in vitro . The differentiation of HL-60 cells was evaluated by light and electron microscopy to observe morphological changes , by chemilumi-nence to detect phagocytosis and by tumorigene-sis in nude mice to determine malignancy . The cytotoxical effect of isoverbascoside on HL-60 cells was examined by trypan blue excluding staining and electron microscopy. The influence of isoverbascoside on cell cycle was measured by flow cytometry. Granular differentiation of HL-60 cells was induced by isoverbascoside at 20-25μmol/L within 1-3 days as the results of morphological changes , enhancement of phagocytosis and decreasing of tumorigenesis . Strong cy-totoxicity was evidenced in HL-60 cells treated by isoverbascoside at 30-35μmol/L. HL-60 cells treated by isoverbascoside at 20μmol/L were delayed at G1 phase at 12 hours and G2/M phase at 72 hours.
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